"68788-8692-2" National Drug Code (NDC)

Ciprofloxacin 20 TABLET in 1 BOTTLE (68788-8692-2)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-8692-2
Package Description20 TABLET in 1 BOTTLE (68788-8692-2)
Product NDC68788-8692
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofolxacin
Dosage FormTABLET
UsageORAL
Start Marketing Date20240610
Marketing Category NameANDA
Application NumberANDA208921
ManufacturerPreferred Pharmaceuticals Inc.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]

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